Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Assess genome assembly quality using QUAST for contiguity metrics and BUSCO for completeness. Essential for evaluating assembly success and comparing assemblers. Use when evaluating assembly completeness and quality.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Reference examples tested with: BUSCO 5.5+, QUAST 5.2+, SPAdes 3.15+, pandas 2.2+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signatures<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Assess my genome assembly quality" → Evaluate assembly contiguity (N50, total length, misassemblies) and gene completeness using conserved single-copy orthologs.
quast assembly.fa -r reference.fa (contiguity), busco -i assembly.fa -l lineage (completeness)| Metric | Good Assembly |
|---|---|
| N50 | High (relative to genome) |
| L50 | Low |
| Contigs | Few |
| Misassemblies | 0 (with reference) |
| BUSCO Complete | >95% |
| BUSCO Duplicated | <5% (unless polyploid) |
conda install -c bioconda quast
quast.py assembly.fasta -o quast_output
quast.py assembly.fasta -r reference.fasta -o quast_output
quast.py assembly1.fa assembly2.fa assembly3.fa -o comparison
| Option | Description |
|---|---|
-o | Output directory |
-r | Reference genome |
-g | Gene annotations (GFF) |
-t | Threads |
-m | Min contig length (default: 500) |
--large | For large genomes (>100Mb) |
--fragmented | For highly fragmented assemblies |
--scaffolds | Input is scaffolds (includes N-gaps) |
quast.py assembly.fasta -r reference.fasta -g genes.gff -o quast_output
quast.py --large assembly.fasta -o quast_output -t 16
quast_output/
├── report.txt # Summary statistics
├── report.html # Interactive report
├── report.tsv # Tab-separated stats
├── icarus.html # Contig viewer
└── aligned_stats/ # If reference provided
| Metric | Description |
|---|---|
| Total length | Sum of contig lengths |
| # contigs | Number of contigs (>= min length) |
| Largest contig | Length of largest contig |
| N50 | 50% of assembly in contigs >= this length |
| N90 | 90% of assembly in contigs >= this length |
| L50 | Number of contigs comprising N50 |
| GC % | GC content |
| # misassemblies | With reference: structural errors |
| Genome fraction | With reference: % of reference covered |
conda install -c bioconda busco
busco -i assembly.fasta -m genome -l bacteria_odb10 -o busco_output
| Option | Description |
|---|---|
-i | Input assembly |
-m | Mode: genome, proteins, transcriptome |
-l | Lineage dataset |
-o | Output name |
-c | CPU threads |
--auto-lineage | Auto-detect lineage |
--offline | Use downloaded datasets only |
--list-datasets | List available lineages |
busco --list-datasets
| Lineage | Use For |
|---|---|
| bacteria_odb10 | Bacteria |
| archaea_odb10 | Archaea |
| eukaryota_odb10 | General eukaryote |
| fungi_odb10 | Fungi |
| metazoa_odb10 | Animals |
| vertebrata_odb10 | Vertebrates |
| mammalia_odb10 | Mammals |
| viridiplantae_odb10 | Plants |
| saccharomycetes_odb10 | Yeasts |
busco -i assembly.fasta -m genome --auto-lineage -o busco_output
busco_output/
├── short_summary.txt # Quick summary
├── full_table.tsv # All BUSCO results
├── missing_busco_list.tsv # Missing genes
└── busco_sequences/ # BUSCO gene sequences
C:98.5%[S:97.0%,D:1.5%],F:0.5%,M:1.0%,n:4085
C - Complete (total)
S - Single-copy
D - Duplicated
F - Fragmented
M - Missing
n - Total BUSCO groups
| Quality | Complete | Missing |
|---|---|---|
| Excellent | >95% | <2% |
| Good | >90% | <5% |
| Acceptable | >80% | <10% |
| Poor | <80% | >10% |
Goal: Run a comprehensive assembly quality assessment combining contiguity and completeness metrics.
Approach: Execute QUAST for contiguity statistics and BUSCO for gene completeness, optionally with a reference genome.
#!/bin/bash
set -euo pipefail
ASSEMBLY=$1
REFERENCE=${2:-}
LINEAGE=${3:-bacteria_odb10}
OUTDIR=${4:-assembly_qc}
mkdir -p $OUTDIR
echo "=== Assembly QC ==="
# QUAST
echo "Running QUAST..."
if [ -n "$REFERENCE" ]; then
quast.py $ASSEMBLY -r $REFERENCE -o ${OUTDIR}/quast -t 8
else
quast.py $ASSEMBLY -o ${OUTDIR}/quast -t 8
fi
# BUSCO
echo "Running BUSCO..."
busco -i $ASSEMBLY -m genome -l $LINEAGE -o busco_run -c 8
mv busco_run ${OUTDIR}/busco
# Summary
echo ""
echo "=== QUAST Summary ==="
cat ${OUTDIR}/quast/report.txt
echo ""
echo "=== BUSCO Summary ==="
cat ${OUTDIR}/busco/short_summary*.txt
echo ""
echo "Reports saved to $OUTDIR"
Goal: Evaluate multiple assemblies side-by-side to select the best one.
Approach: Run QUAST with multiple input assemblies and labeled names, then generate BUSCO comparison plots.
quast.py \
spades_assembly.fa \
flye_assembly.fa \
canu_assembly.fa \
-r reference.fa \
-l "SPAdes,Flye,Canu" \
-o assembly_comparison
# Run BUSCO on each assembly
for asm in spades.fa flye.fa canu.fa; do
name=$(basename $asm .fa)
busco -i $asm -m genome -l bacteria_odb10 -o busco_${name}
done
# Generate comparison plot
generate_plot.py -wd . busco_spades busco_flye busco_canu
Goal: Programmatically extract assembly metrics from QUAST reports.
Approach: Read the tab-separated report.tsv file and transpose it for easy metric access.
import pandas as pd
def parse_quast(report_tsv):
'''Parse QUAST report.tsv file.'''
df = pd.read_csv(report_tsv, sep='\t', index_col=0)
return df.T
stats = parse_quast('quast_output/report.tsv')
print(f"N50: {stats['N50'].values[0]}")
print(f"Total length: {stats['Total length'].values[0]}")
print(f"# contigs: {stats['# contigs'].values[0]}")
Goal: Programmatically extract BUSCO completeness metrics from summary files.
Approach: Parse the short_summary.txt file using regex to capture completeness, duplication, fragmentation, and missing percentages.
import re
def parse_busco_summary(summary_file):
'''Parse BUSCO short summary.'''
with open(summary_file) as f:
text = f.read()
pattern = r'C:(\d+\.\d+)%\[S:(\d+\.\d+)%,D:(\d+\.\d+)%\],F:(\d+\.\d+)%,M:(\d+\.\d+)%,n:(\d+)'
match = re.search(pattern, text)
if match:
return {
'complete': float(match.group(1)),
'single': float(match.group(2)),
'duplicated': float(match.group(3)),
'fragmented': float(match.group(4)),
'missing': float(match.group(5)),
'total': int(match.group(6))
}
return None
result = parse_busco_summary('busco_output/short_summary.txt')
print(f"Complete: {result['complete']}%")
Goal: Assess metagenome assembly quality accounting for multiple reference genomes.
Approach: Run MetaQUAST which automatically identifies reference genomes and reports per-genome metrics.
metaquast.py metagenome_assembly.fa -o metaquast_output -t 16
まだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
日本語の概要は準備中です。原文の説明を表示しています。
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
日本語の概要は準備中です。原文の説明を表示しています。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
日本語の概要は準備中です。原文の説明を表示しています。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
日本語の概要は準備中です。原文の説明を表示しています。
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
日本語の概要は準備中です。原文の説明を表示しています。